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威尔逊病所致急性肝衰竭的急诊ABO血型不相容活体供肝肝移植

Emergency ABO-incompatible living donor liver transplantation in Wilson disease-induced acute liver failure.

作者信息

Valamparampil Joseph J, Sachan Deepti, Shanmugam Naresh, Reddy Srinivas Mettu, Rela Mohamed

机构信息

Institute of Liver Disease and Transplantation, Chennai, Tamil Nadu, India.

Department of Transfusion Medicine, Bharat Institute of Higher Education and Research, Dr. Rela Institute and Medical Centre, Chennai, Tamil Nadu, India.

出版信息

Asian J Transfus Sci. 2023 Jan-Jun;17(1):128-130. doi: 10.4103/ajts.ajts_55_21. Epub 2022 May 26.

Abstract

We report the clinical outcome of an emergency ABO incompatible-liver transplantation (LT) for an 8-year-old child with Wilson's disease-induced acute liver failure. The pretransplant anti-A antibody titer was 1:64, and hence he underwent three cycles of conventional plasma exchange as pretransplant liver supportive treatment for deranged coagulopathy and liver function followed by one cycle of immunoadsorption (IA) prior to LT. The posttransplant immunosuppression consisted of rituximab, tacrolimus, mycophenolate mofetil, and corticosteroid. The patient had anti-A isoagglutinin rebound with elevated aminotransferases levels from postoperative day 7 for which he was restarted on IA plasmapheresis, but antibody titers did not decrease. Hence, he was switched to conventional plasmapheresis (CP) with which anti-A antibody titers decreased. The total dose of rituximab (150 milligrams/square meter of body surface area) was given in two divided doses of 75 mg at D-1 and D + 8 which was much less than the dose conventionally advocated (375 milligrams/square meter of body surface area). He is clinically well with good graft function without rejection after 1 year of follow-up. This case illustrates that IA and CP in conjunction with adequate immunosuppression is a viable approach in emergency ABO-incompatible-LT in Wilson disease-induced acute liver failure.

摘要

我们报告了一名8岁患有威尔逊病所致急性肝衰竭儿童接受紧急ABO血型不相容肝移植(LT)的临床结果。移植前抗A抗体滴度为1:64,因此他在LT前接受了三个周期的传统血浆置换,作为针对凝血功能障碍和肝功能紊乱的移植前肝脏支持治疗,随后在LT前进行了一个周期的免疫吸附(IA)。移植后免疫抑制包括利妥昔单抗、他克莫司、霉酚酸酯和皮质类固醇。患者术后第7天出现抗A同种凝集素反弹,转氨酶水平升高,为此他重新开始IA血浆置换,但抗体滴度未降低。因此,他改用传统血浆置换(CP),抗A抗体滴度随之降低。利妥昔单抗的总剂量(150毫克/平方米体表面积)分两次给药,分别在D-1和D+8时给予75毫克,远低于传统推荐剂量(375毫克/平方米体表面积)。随访1年后,他临床状况良好,移植肝功能良好,无排斥反应。该病例表明,IA和CP联合适当的免疫抑制是威尔逊病所致急性肝衰竭紧急ABO血型不相容LT的一种可行方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c439/10180780/db664f7ae2ba/AJTS-17-128-g001.jpg

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